Fenofibrate interactions
Full monograph for FenofibrateCheck it against another medicine
Medicines
518 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Amlodipine Besilate + Atorvastatin | Major | Others · Unknown | Severe myopathy and rhabdomyolysis have been reported during concomitant use of HMG-CoA reductase inhibitors and fibric acid derivatives, especially…2 documented mechanisms | 49 sources — open the full entry |
| Atorvastatin + Ezetimibe | Major | Others · Synergy | Severe myopathy and rhabdomyolysis have been reported during concomitant use of HMG-CoA reductase inhibitors and fibric acid derivatives, especially…2 documented mechanisms | 50 sources — open the full entry |
| Atorvastatin Calcium | Major | Others | Severe myopathy and rhabdomyolysis have been reported during concomitant use of HMG-CoA reductase inhibitors and fibric acid derivatives, especially… | 49 sources — open the full entry |
| Citalopram Hydrobromide | Major | Metabolism | Coadministration with CYP450 2C19 inhibitors may increase the plasma concentrations of citalopram, which is partially metabolized by the isoenzyme. Cases of QT… | 9 sources — open the full entry |
| Fluvastatin | Major | Others | Severe myopathy and rhabdomyolysis have been reported during concomitant use of HMG-CoA reductase inhibitors and fibric acid derivatives, especially… | 49 sources — open the full entry |
| Leflunomide | Major | Synergy | The recent, concomitant, or subsequent use (without the recommended leflunomide washout period or procedure) of other agents known to induce hepatotoxicity may… | 3 sources — open the full entry |
| Mavacamten | Major | Metabolism | Coadministration with inhibitors of CYP450 2C19 or CYP450 3A4 may increase the plasma concentrations of mavacamten. | 1 sources — open the full entry |
| Pitavastatin Calcium | Major | Others | Severe myopathy and rhabdomyolysis have been reported during concomitant use of HMG-CoA reductase inhibitors and fibric acid derivatives, especially… | 49 sources — open the full entry |
| Pravastatin Sodium | Major | Others | Severe myopathy and rhabdomyolysis have been reported during concomitant use of HMG-CoA reductase inhibitors and fibric acid derivatives, especially… | 49 sources — open the full entry |
| Rosuvastatin + Ezetimibe | Major | Others · Synergy | Severe myopathy and rhabdomyolysis have been reported during concomitant use of HMG-CoA reductase inhibitors and fibric acid derivatives, especially…2 documented mechanisms | 50 sources — open the full entry |
| Rosuvastatin Calcium | Major | Others | Severe myopathy and rhabdomyolysis have been reported during concomitant use of HMG-CoA reductase inhibitors and fibric acid derivatives, especially… | 49 sources — open the full entry |
| Simvastatin | Major | Others | Severe myopathy and rhabdomyolysis have been reported during concomitant use of HMG-CoA reductase inhibitors and fibric acid derivatives, especially… | 49 sources — open the full entry |
| Warfarin Sodium | Major | Distribution | Fibric acid derivatives may enhance the hypoprothrombinemic effect of coumarin-type oral anticoagulants. The mechanism may involve displacement of… | 46 sources — open the full entry |
| Avatrombopag | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Bempedoic acid + Ezetimibe | Moderate | Synergy | Concomitant use of ezetimibe may potentiate the risk of cholelithiasis associated with fenofibrate and other fibrates. Fibrates can increase cholesterol… | 1 sources — open the full entry |
| Biphasic Insulin Aspart | Moderate | Synergy | The hypoglycemic effect of insulin may be potentiated by certain drugs, including ACE inhibitors, angiotensin receptor blockers (ARBs), 4-aminoquinolines… | 86 sources — open the full entry |
| Bosentan Monohydrate | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Carisoprodol | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Cilostazol | Moderate | Metabolism | Coadministration with inhibitors of CYP450 3A4 and/or 2C19 may increase the plasma concentrations of cilostazol and or its pharmacologically active… | 11 sources — open the full entry |
| Clobazam | Moderate | Metabolism | Coadministration of clobazam with inhibitors of CYP450 2C19 may significantly increase the plasma concentrations of its active metabolite, N-desmethylclobazam… | 7 sources — open the full entry |
| Clopidogrel + Aspirin | Moderate | Metabolism · Unknown | Coadministration with inhibitors of CYP450 2C19 may reduce the efficacy of clopidogrel, whose antiplatelet effect is dependent in part on bioactivation by the…2 documented mechanisms | 21 sources — open the full entry |
| Clopidogrel Bisulphate | Moderate | Metabolism | Coadministration with inhibitors of CYP450 2C19 may reduce the efficacy of clopidogrel, whose antiplatelet effect is dependent in part on bioactivation by the… | 21 sources — open the full entry |
| Clozapine | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Colchicine | Moderate | Synergy | Limited data suggest that coadministration of colchicine and fibric acid derivatives may increase the risk of myopathy. The mechanism of interaction has not… | 21 sources — open the full entry |
| Cyclophosphamide | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Cyclosporine (Oral) | Moderate | Excretion | The concomitant use of cyclosporine and fibric acid derivatives may increase the risk of nephrotoxicity. Fibrates are primarily eliminated by the kidneys and… | 20 sources — open the full entry |
| Dapsone | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Dexibuprofen | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Diclofenac Diethylamine + Mephenesin + Menthol + Methyl Salicylate + Turpentine Oil | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Diclofenac Potassium | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Diclofenac Sodium | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Diclofenac Sodium + Lidocaine Hydrochloride | Moderate | Metabolism · Unknown | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9…2 documented mechanisms | 37 sources — open the full entry |
| Diclofenac Sodium + Methyl Salicylate + Linseed Oil + Menthol | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Diclofenac Sodium + Misoprostol | Moderate | Metabolism · Unknown | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9…2 documented mechanisms | 37 sources — open the full entry |
| Efavirenz | Moderate | Synergy | Coadministration of efavirenz with other agents known to induce hepatotoxicity may potentiate the risk of liver injury. Efavirenz has been associated with… | 7 sources — open the full entry |
| Epirubicin Hydrochloride | Moderate | Synergy | The concomitant or sequential use of epirubicin with agents known to induce hepatotoxicity may potentiate the risk of liver injury. Epirubicin undergoes… | 4 sources — open the full entry |
| Escitalopram Oxalate | Moderate | Metabolism | Coadministration with inhibitors of CYP450 2C19 may increase the plasma concentrations of escitalopram, which is primarily metabolized by the isoenzyme. High… | 18 sources — open the full entry |
| EsomeprazolebaseMUPS preparation | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Esomeprazole + Amoxicillin + Clarithromycin | Moderate | Metabolism · Unknown | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9…3 documented mechanisms | 37 sources — open the full entry |
| Ezetimibe | Moderate | Synergy | Concomitant use of ezetimibe may potentiate the risk of cholelithiasis associated with fenofibrate and other fibrates. Fibrates can increase cholesterol… | 1 sources — open the full entry |
| Flibanserin | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Fosphenytoin Sodium | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Glibenclamide | Moderate | Synergy | The hypoglycemic effect of insulin secretagogues (e.g., sulfonylureas, meglitinides) may be potentiated by certain drugs, including ACE inhibitors… | 112 sources — open the full entry |
| Glimepiride | Moderate | Synergy | The hypoglycemic effect of insulin secretagogues (e.g., sulfonylureas, meglitinides) may be potentiated by certain drugs, including ACE inhibitors… | 112 sources — open the full entry |
| Glimepiride + Metformin | Moderate | Synergy · Unknown | The hypoglycemic effect of insulin secretagogues (e.g., sulfonylureas, meglitinides) may be potentiated by certain drugs, including ACE inhibitors…2 documented mechanisms | 112 sources — open the full entry |
| Glipizide | Moderate | Synergy | The hypoglycemic effect of insulin secretagogues (e.g., sulfonylureas, meglitinides) may be potentiated by certain drugs, including ACE inhibitors… | 112 sources — open the full entry |
| Glipizide + Metformin Hydrochloride | Moderate | Synergy · Unknown | The hypoglycemic effect of insulin secretagogues (e.g., sulfonylureas, meglitinides) may be potentiated by certain drugs, including ACE inhibitors…2 documented mechanisms | 112 sources — open the full entry |
| IbuprofenOralTopical | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
| Ibuprofen + Paracetamol | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9…2 documented mechanisms | 37 sources — open the full entry |
| IndomethacinOralRectal | Moderate | Metabolism | Coadministration with fenofibrate may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 2C19, 2A6, and 2C9… | 37 sources — open the full entry |
Conditions
Conditions in which Fenofibrate needs care, as documented in this source.
Cholelithiasis
MajorThe use of fibric acid derivatives is contraindicated in patients with gallbladder disease. A significantly increased incidence of cholelithiasis has been observed in patients treated with the fibric acid derivative, clofibrate, presumably because of increased cholesterol excretion into the bile. Based on two separate studies (the WHO study and the Coronary Drug Project study), clofibrate use was associated with twice the risk of developing cholelithiasis and cholecystitis requiring surgery. Due to their structural and pharmacologic similarities, use of other fibric acid derivatives may be expected to carry the same risk.
7 sources
- "Product Information. Lopid (gemfibrozil)." Parke-Davis (2002):
- Blane GF "Comparative toxicity and safety profile of fenofibrate and other fibric acid derivatives." Am J Med 83 (1987): 26-36
- Roberts WC "Safety of fenofibrate--US and worldwide experience." Cardiology 76 (1989): 169-79
- "Product Information. Atromid-S (clofibrate)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Tricor (fenofibrate)." Abbott Pharmaceutical (2001):
- "Product Information. Trilipix (fenofibric acid)." Abbott Pharmaceutical (2008):
- "Product Information. Fibricor (fenofibric acid)." AR Scientific Inc (2009):
Hypolipoproteinemias
MajorThere have been reports of severe decreases in HDL cholesterol (HDL-C) levels (as low as 2 mg/dL) occurring in diabetic and non-diabetic patients initiated on fibric acid derivatives therapy. The decrease has been reported to occur within 2 weeks to years after initiation of therapy. It is recommended that HDL-C levels be checked within the first few months after initiation therapy and if a severely depressed HDL-C level is detected, therapy with these agents should be withdrawn. Monitor HDL-C level until it has returned to baseline, and therapy with these agents should not be re-initiated in these patients.
4 sources
- "Product Information. Lopid (gemfibrozil)." Parke-Davis (2002):
- Thompson CH, Irish A, Kemp GJ, Taylor DJ, Radda GK "Skeletal muscle metabolism before and after gemfibrozil treatment in dialysed patients with chronic renal failure." Clin Nephrol 45 (1996): 386-9
- Gorriz JL, Sancho A, Lopezmartin JM, Alcoy E, Catalan C, Pallardo LM "Rhabdomyolysis and acute renal failure associated with gemfibrozil therapy." Nephron 74 (1996): 437-8
- "Product Information. Tricor (fenofibrate)." Abbott Pharmaceutical (2001):
Kidney Diseases
MajorThe use of fibric acid derivatives is contraindicated in patients with significantly impaired renal function. The rate of clearance of fenofibric acid has been shown to decrease substantially when CrCl is below 50 mL/min, with drug accumulation during chronic dosing. Increased adverse effects, including rhabdomyolysis (with or without secondary renal failure) and severe hyperkalemia, have been associated with the use of fibric acid derivatives in patients with renal insufficiency. Therapy with these agents should be administered cautiously in patients with mild or moderate renal impairment. Close clinical monitoring is recommended during therapy.
12 sources
- Pokroy N, Ress S, Gregory MC "Clofibrate-induced complications in renal disease: a case report." S Afr Med J 52 (1977): 806-8
- Goldman JA, Fishman AB, Lee JE, Johnson RJ "The role of cholesterol-lowering agents in drug-induced rhabdomyolysis and polymyositis ." Arthritis Rheum 32 (1989): 358-9
- Chapman MJ "Pharmacology of fenofibrate." Am J Med 83 (1987): 21-5
- Weil A, Caldwell J, Strolin-Benedetti M "The metabolism and disposition of 14C-fenofibrate in human volunteers." Drug Metab Dispos 18 (1990): 115-20
- Balfour JA, McTavish D, Heel RC "Fenofibrate. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic use in dyslipidaemia." Drugs 40 (1990): 260-90
- Dealava E, Sola JJ, Lozano MD, Pardomindan FJ "Rhabdomyolysis and acute renal failure in a heart transplant recipient treated with hypolipemiants." Nephron 66 (1994): 242-3
- Thompson CH, Irish A, Kemp GJ, Taylor DJ, Radda GK "Skeletal muscle metabolism before and after gemfibrozil treatment in dialysed patients with chronic renal failure." Clin Nephrol 45 (1996): 386-9
- Gorriz JL, Sancho A, Lopezmartin JM, Alcoy E, Catalan C, Pallardo LM "Rhabdomyolysis and acute renal failure associated with gemfibrozil therapy." Nephron 74 (1996): 437-8
Show all 12 sourcesShow fewer sources
- "Product Information. Tricor (fenofibrate)." Abbott Pharmaceutical (2001):
- Miller DB, Spence JD "Clinical pharmacokinetics of fibric acid derivatives (fibrates)." Clin Pharmacokinet 34 (1998): 155-62
- "Product Information. Trilipix (fenofibric acid)." Abbott Pharmaceutical (2008):
- "Product Information. Fibricor (fenofibric acid)." AR Scientific Inc (2009):
Liver Cirrhosis, Biliary
MajorThe use of fibric acid derivatives is contraindicated in patients with primary biliary cirrhosis. These agents may further raise the already elevated cholesterol in these patients.
5 sources
- "Product Information. Lopid (gemfibrozil)." Parke-Davis (2002):
- "Product Information. Atromid-S (clofibrate)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Tricor (fenofibrate)." Abbott Pharmaceutical (2001):
- "Product Information. Trilipix (fenofibric acid)." Abbott Pharmaceutical (2008):
- "Product Information. Fibricor (fenofibric acid)." AR Scientific Inc (2009):
Liver Diseases
MajorThe use of fibric acid derivatives is contraindicated in patients with active liver disease or unexplained, persistent elevations of serum transaminases. Fibric acid derivatives therapy is associated with dose-related hepatotoxicity, including biochemical abnormalities of liver function, hepatitis (hepatocellular, chronic active, as well as cholestatic) and, rarely, cirrhosis. Postmarketing cases of severe drug-induced liver injury, including liver transplantation and death, have been reported. Therapy with these agents should be administered cautiously in patients with a history of liver disease and/or heavy alcohol use. Liver function tests, including serum transaminase levels and total bilirubin, should be performed at baseline and periodically throughout the duration of therapy. Therapy should be discontinued if signs or symptoms of liver injury develop or if elevated enzyme levels persist (ALT or AST greater than 3 times the upper limit of normal, or if accompanied by elevation of bilirubin). Do not restart therapy if there is no alternative explanation for the liver injury.
9 sources
- Cayen MN "Disposition, metabolism and pharmacokinetics of antihyperlipidemic agents in laboratory animals and man." Pharmacol Ther 29 (1985): 157-204
- Chapman MJ "Pharmacology of fenofibrate." Am J Med 83 (1987): 21-5
- Weil A, Caldwell J, Strolin-Benedetti M "The metabolism and disposition of 14C-fenofibrate in human volunteers." Drug Metab Dispos 18 (1990): 115-20
- Balfour JA, McTavish D, Heel RC "Fenofibrate. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic use in dyslipidaemia." Drugs 40 (1990): 260-90
- "Product Information. Tricor (fenofibrate)." Abbott Pharmaceutical (2001):
- Adkins JC, Faulds D "Micronised fenofibrate: a review of its pharmacodynamic properties and clinical efficacy in the management of dyslipidaemia." Drugs 54 (1997): 615-33
- Miller DB, Spence JD "Clinical pharmacokinetics of fibric acid derivatives (fibrates)." Clin Pharmacokinet 34 (1998): 155-62
- "Product Information. Trilipix (fenofibric acid)." Abbott Pharmaceutical (2008):
Show all 9 sourcesShow fewer sources
- "Product Information. Fibricor (fenofibric acid)." AR Scientific Inc (2009):
Rhabdomyolysis
MajorSevere myopathy, including rhabdomyolysis with acute renal failure secondary to myoglobinuria, has been reported rarely with the use of fibric acid derivatives. The myopathy may be dose-related and is characterized by muscle aches and/or weakness in conjunction with increases in creatine phosphokinase (CPK) values exceeding 10 times the upper limit of normal. Therapy with fibric acid derivatives should be administered cautiously in patients with preexisting myopathy or a myoneural disorder, since it may delay the recognition or confound the diagnosis of a drug-induced musculoskeletal effect. Patients should be advised to report promptly any unusual muscle pain, tenderness or weakness, particularly if accompanied by malaise or fever. Periodic CPK determinations may be considered in some patients, although the value of such monitoring is uncertain. Therapy should be withdrawn if markedly elevated CPK levels occur or if drug-related myopathy is diagnosed or suspected.
23 sources
- Pokroy N, Ress S, Gregory MC "Clofibrate-induced complications in renal disease: a case report." S Afr Med J 52 (1977): 806-8
- Abourizk N, Khalil BA, Bahuth N, Afifi AK "Clofibrate-induced muscular syndrome. Report of a case with clinical, electromyographic and pathologic observations." J Neurol Sci 42 (1979): 1-9
- Rush P, Baron M, Kapusta M "Clofibrate myopathy: a case report and a review of the literature." Semin Arthritis Rheum 15 (1986): 226-9
- Goldman JA, Fishman AB, Lee JE, Johnson RJ "The role of cholesterol-lowering agents in drug-induced rhabdomyolysis and polymyositis ." Arthritis Rheum 32 (1989): 358-9
- Fusella J, Strosberg JM "Polymyositis exacerbated by gemfibrozil ." J Rheumatol 17 (1990): 572-3
- Pierce LR, Wysowski DK, Gross TP "Myopathy and rhabdomyolysis associated with lovastatin-gemfibrozil combination therapy." JAMA 264 (1990): 71-5
- Chow LT, Chow WH "Acute compartment syndrome: an unusual presentation of gemfibrozil induced myositis." Med J Aust 158 (1993): 48-9
- "Product Information. Lopid (gemfibrozil)." Parke-Davis (2002):
Show all 23 sourcesShow fewer sources
- Blane GF "Comparative toxicity and safety profile of fenofibrate and other fibric acid derivatives." Am J Med 83 (1987): 26-36
- Roberts WC "Safety of fenofibrate--US and worldwide experience." Cardiology 76 (1989): 169-79
- Dealava E, Sola JJ, Lozano MD, Pardomindan FJ "Rhabdomyolysis and acute renal failure in a heart transplant recipient treated with hypolipemiants." Nephron 66 (1994): 242-3
- Shepherd J "Fibrates and statins in the treatment of hyperlipidaemia: an appraisal of their efficacy and safety." Eur Heart J 16 (1995): 5-13
- Thompson CH, Irish A, Kemp GJ, Taylor DJ, Radda GK "Skeletal muscle metabolism before and after gemfibrozil treatment in dialysed patients with chronic renal failure." Clin Nephrol 45 (1996): 386-9
- "Product Information. Atromid-S (clofibrate)." Wyeth-Ayerst Laboratories (2001):
- Gorriz JL, Sancho A, Lopezmartin JM, Alcoy E, Catalan C, Pallardo LM "Rhabdomyolysis and acute renal failure associated with gemfibrozil therapy." Nephron 74 (1996): 437-8
- "Product Information. Tricor (fenofibrate)." Abbott Pharmaceutical (2001):
- Duell PB, Connor WE, Illingworth DR "Rhabdomyolysis after taking atorvastatin with gemfibrozil." Am J Cardiol 81 (1998): 368-9
- Kirchgassler KU, Schmitz H, Bach G "Effectiveness and tolerability of 12-week treatment with micronised fenofibrate 200mg in a drug-monitoring programme involving 9884 patients with dyslipidaemia." Clin Drug Invest 15 (1998): 197-204
- Iliadis EA, Rosenson RS "Long-term safety of pravastatin-gemfibrozil therapy in mixed hyperlipidemia." Clin Cardiol 22 (1999): 25-8
- van Puijenbroek EP, Du Buf-Vereijken PW, Spooren PF, van Doormaal JJ "Possible increased risk of rhabdomyolysis during concomitant use of simvastatin and gemfibrozil." J Intern Med 240 (1996): 403-4
- Pogson GW, Kindred LH, Carper BG "Rhabdomyolysis and renal failure associated with cerivastatin-gemfibrozil combination therapy." Am J Cardiol 83 (1999): 1146
- "Product Information. Trilipix (fenofibric acid)." Abbott Pharmaceutical (2008):
- "Product Information. Fibricor (fenofibric acid)." AR Scientific Inc (2009):
Hematologic Diseases
ModerateMild to moderate hemoglobin, hematocrit and white blood cell decreases have been observed in patients following initiation of fibric acid derivatives therapy. However, these levels stabilize during long-term administration. Thrombocytopenia and agranulocytosis have been reported in individuals treated with these agents. Caution is recommended when treating patients predisposed to hematologic changes. Periodic monitoring of red and white blood cell counts is recommended during the first 12 months of therapy.
4 sources
- "Product Information. Lopid (gemfibrozil)." Parke-Davis (2002):
- Thompson CH, Irish A, Kemp GJ, Taylor DJ, Radda GK "Skeletal muscle metabolism before and after gemfibrozil treatment in dialysed patients with chronic renal failure." Clin Nephrol 45 (1996): 386-9
- Gorriz JL, Sancho A, Lopezmartin JM, Alcoy E, Catalan C, Pallardo LM "Rhabdomyolysis and acute renal failure associated with gemfibrozil therapy." Nephron 74 (1996): 437-8
- "Product Information. Tricor (fenofibrate)." Abbott Pharmaceutical (2001):